View drug registration information details.
| Items | Registration information |
|---|
| ID | 844 |
|---|
| No | 844 |
|---|
| Brand Name | ATROPINE SULFATE |
|---|
| Ingredients | ATROPINE SULFATE 0.6MG/ML |
|---|
| Dosage Form | INJECTION |
|---|
| Primary Packaging | AMPOULE |
|---|
| Storage | ROOM TEMPERATURE |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | 10 AMP OF 1ML/BOX |
|---|
| Dispensing Category | Prescription only |
|---|
| ATC Classification | A03BA01 |
|---|
| Pharmaceutical Class | ANTISPASMODICS |
|---|
| Indications | ANTISPAMODIC |
|---|
| Contraindications | GLAUCOMA OR INCREASED INTRAOCULAR PRESSURE, PROSTATIC HYPERTROPHY, CIRRHOSIS |
|---|
| Side Effects | DRY MOUTH, BLURRED VISION, TACHYCARDIA, EXCITEMENT |
|---|
| Unit Price | - |
|---|
| EDL |
Yes |
|---|
| Description | CLEAR & STERILE LIQUID |
|---|
| Note | |
|---|
| License Owner | FACTORY NO.2 |
|---|
| Manufacturer | FACTORY NO. 2 |
|---|
| Country | LAO PDR |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | 2016-08-07 |
|---|
| FDD Registration No | 03 L 0051/92 |
|---|
| FDD Registration Date | 2022-04-18 |
|---|
| Expiry Date | 2025-04-17 |
|---|
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